Classifications

• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
  • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
  • G03G5/02—Charge-receiving layers
  • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
  • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
  • G03G5/0664—Dyes
  • G03G5/0666—Dyes containing a methine or polymethine group
  • G03G5/0668—Dyes containing a methine or polymethine group containing only one methine or polymethine group
  • G03G5/067—Dyes containing a methine or polymethine group containing only one methine or polymethine group containing hetero rings
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/0008—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain
  • C09B23/0025—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain the substituent being bound through an oxygen atom
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/0008—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain
  • C09B23/0033—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain the substituent being bound through a sulfur atom
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/0008—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain
  • C09B23/005—Methine or polymethine dyes, e.g. cyanine dyes substituted on the polymethine chain the substituent being a COOH and/or a functional derivative thereof
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/06—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups three >CH- groups, e.g. carbocyanines
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/08—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines
  • C09B23/083—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines five >CH- groups
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
  • C09B23/08—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines
  • C09B23/086—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups more than three >CH- groups, e.g. polycarbocyanines more than five >CH- groups
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
  • C09B23/105—The polymethine chain containing an even number of >CH- groups two >CH- groups
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
  • C09B23/10—The polymethine chain containing an even number of >CH- groups
  • C09B23/107—The polymethine chain containing an even number of >CH- groups four >CH- groups

Definitions

• Such process is conducted by reacting the active methylene group containing compounds with an in situ or a preformed intermediate produced by the reaction of ethyl chloroformate and an anilinovinyl, polyvinyl or methylene quaternary ammonium compound.
• the present invention is directed to a novel process of producing dyes, i.e. cyanine dyes; more particularly, the process of the present invention is directed to an improved process for producing such dyes through the employment of an N-phenyl-N-vinyl urethane intermediate compound or its analogues.
• Cyanine dyes are well known as optical sensitizers for silver halide emulsions, photoconducting compositions, and similar materials. Generally, such cyanine dyes, including carbocyanine dyes, merocyanine dyes and chainsubstituted cyanine dyes have been prepared by the reaction of two intermediates, which during the course of the reaction result in the elimination of simple molecules such as mercaptans, alcohols, water, acids, aniline or acylanilide.
• One of the intermediates generally employed in the production of the optical sensitizing cyanine dyes is a compound containing an active methyl group which reacts through the formation of a methylene base as follows:
• the othe rreactant in the production of the optical sensitizing cyanine dyes can be a nitrogenous quaternary ammonium salt which contains a proton seeking atom or group in th 6 or 7 position relative to the nitrogen of a nitrogenous hetero nucleus through a vinyl or polyvinyl or methylenic linkage.
• This type of reactant is exemplified by the following structure:
• Y and Y which may be the same or different, are selected from O, N, C, S, Se atoms, the group of atoms necessary to complete the heterocyclic ring structure of the types previously known to be used in the synthesis of cyanine dyes, particularly those used for the optical sensitization of photographic silver halide emulsions; and
• X which may be the same or different, are anions such as alkyl sulfate, chlorine, bromine, iodine, sulfate, perchlorate, benzenesulfonate, ptoluenesulfonate and other substituted phenyl sulfonates, etc.;
• R and R which may be the same or ditferent, are lower alkyl groups, e.g., methyl, ethyl, n-propyl, isopropyl and the like; substituted alkyl group, e.g., hydroxymethyl, hydroxyethyl, hydroxy
• ethyl chloroformate as a reagent in the dye condensations of anilinovinyl, polyvinyl or methylene intermediates with compounds containing active methyl and methylene groups whereby in the formation of the desired cyanine, merocyanine or oxonol dyes, a phenyl urethane group is eliminated.
• cyanine dyes in general including those known to be used for the optical sensitization of silver halide emulsions, etc. can be advantageously prepared in a manner essentially free from the objectionable side reactions due to fragmentation, multiple condensation or decomposition, etc., by employing in lieu of the conventional acylaniliovinyl, polyvinyl or methylene, e.g., acetanilovinyl, polyvinyl or methylene moiety generally employed in the production of such cyanine dyes by re- 3 action with the active methyl or active methylene containing compound, a compound containing an N-phenyl-N- vinyl polyvinyl or methylene urethane grouping.
• the procedure of the present invention comprises an improved process for the production of cyanine-like dyes, such improvement relating for example to the employment of various heterocyclic nitrogeneous quaternary ammonium N-phenyl-N-vinyl urethanes, either pre-formed or prepared in situ as intermediates for the preparation of such dyes by the reaction with compounds containing active methyl or methylene groups.
• R represents an alkyl, allyl, hydroxyalkyl, alkoxyalkyl, carboxyalkyl, carboxyalkoxy or aralkyl; group; -A- is a polyvinyl chain of from 1 to 3 vinyl units which may be unsubstituted or substituted by alkyl or aryl, e. g., phenyl, oxyphenyl, thiophenyl and is characterized by the structural formula:
• R and R are hydrogen, lower alkyl, aryl, aryloxy and arylthio; n is 1, 2, or 3, at least one of R and R being hydrogen, R always being hydrogen when n is 2 or 3;
• X is selected from halide, e.g., bromide and iodide, perchorate, sulfate, alkyl sulfate, e.g., methyl sulfate, ethyl sulfate; e.g., benzene sulfonate; sulfo alkyl, e.g., sulfo propyl: substituted phenyl sulfonate, e.g., p-toluenesulfonate and the like;
• Y represents the non-metallic atoms necessary to form a 5- or 6-membered heterocyclic ring system of the type commonly known in cyanine dyes or fused ring derivative thereof; and
• alkyl moiety representing R, R R R R and R is generally a lower alkyl group having from 1 to about 6 carbon atoms.
• suitable alkyl and substituted alkyl groups from R, R and R include:
• n-hexyl ethyl hydroxymethyl n-propyl hydroxyethyl iso-propyl hydroxypropyl n-butyl hydroxybutyl iso-butyl carboxymethyl t-butyl carboxyethyl n-amyl carboxypropyl iso-amyl and the like.
• R, R R R R and R include as representative examples:
• Suitable oxyalkyl radicals for R include as representative examples:
• aromatic rings suitable for R include phenyl and the halogen and lower alkyl substituted phenyl radicals and thienyl.
• suitable heterocyclic rings embraced by the above-described formulae include as representative examples those selected from the group consisting of those of the thiazole series (e.g., thiazole, 4- methylthiazole, 4 phenylthiazole, 5 methylthiazole, 5- phenylthiazole, 4,5 -dimethylthiazole, 4,5-diphenylthiazole, 4-(2-thienyl)thiazole, etc.), those of the benzothiazole series (e.g., benzothiazole, 4-chlorobenzothiazole, S-chlorobenzothiazole, 6-chlorobenzothiazole, 7-chlorobenzothi
• representative heterocyclic rings embraced by the above described general formula include those of the pyrazolone series (e.g., 3 methyl-l-phenyl-S-pyrazolone, l-phenyl-Z-pyrazolone, 1-(2-benzothiazolyl)-3-methyl-5-pyrazolone, etc.) those of the isoxazolone series (e.g., 3-phenyl-5(4H)-isoxazolone, 3-methyl-5(4H)-isoxazolone, etc.), those of the oxidole series, (e.g., 1-alkyl-2,3-dihydro-2-oxindoles, etc.), those of the 2,4,6-triketodehexahydropyrimidine series (e.
• pyrazolone series e.g., 3 methyl-l-phenyl-S-pyrazolone, l-phenyl-Z-pyrazolone, 1-(2-benzothiazolyl)-3-methyl-5-
• the heterocyclic radicals comprising a portion of, the cyclic quaternary ammonium alkene urethanes and cyclic tertiary amidinium alkene urethanes employed as reactants in accordance with the improved process of the present invention are those which comprise a 5- or 6-membered nitrogenous heterocyclic ring system containing in addition to at least one nitrogen atom such other atoms including carbon, hydrogen, oxygen, sulfur, selenium etc. so as to form a heterocyclic nucleus of the type used in the synthesis of mercocyanine or oxanol dyes including those which are used as sensitizers particularly for photographic silver halide emulsions.
• the above exemplary materials illustrate the operable employment of the fused ring derivatives of such heterocyclic radical.
• cyanine dyes i.e., carbocyanine, merocyanine, mesosubstituted carbocyanine, oxanol, chain-substituted polycarbocyanine, etc.
• cyanine dyes i.e., carbocyanine, merocyanine, mesosubstituted carbocyanine, oxanol, chain-substituted polycarbocyanine, etc.
• Such reactants containing an active methylene group correspond generally wherein R, X, and Y are as defined above with respect to the quaternary ammonium and tertiary amidinium alkene urethane reactants employed in accordance with the improved process of the present invention.
• A has the value given above and B is alkyl, hydrogen, lower aryl, e.g., phenyl, substituted phenyl or a heterocyclic nucleus, the latter having the configuration in which R and R and Y and Y respectively, are identical with each other.
• reaction to produce the desired merocyanine dye proceeds smoothly in accordance with the present invention through the elimination of phenyl urethane.
• the urethane materials of the present invention have the capacity to condense into cyanine dyes with little, if any, side reactions as compared with the conventionally employed anilido or acetanilido intermediates, thereby resulting in the improved process of the present invention.
• the use of the N-phenyl-N- vinylpolyvinyl or methylene-urethane containing reactants in accordance with the present invention comprises an improvement in the well known and conventional condensation reaction employed in the production of cyanine merocyanine and oxanol dyes.
• carbocyanine dyes e.g., carbocyanine, merocyanine, oxanol
• the condensation of an active methyl or methylene group containing reactant and an N-phenyl-N-vinyl, polyvinyl or methylene urethane containing reactant, i.e., cyclic quaternary ammonium vinyl or polyvinyl urethane or cyclic tertiary amidinium alkyleneurethane is generally accelerated by the employment of basic condensing agents, such as the trialkyl amines (trimethylamine, triethylamine, tri-n-propylamine, triisopropylamine, tri n butylamine, etc.), N,N-lower dialkylaniline (e.g., N,N-dimethylaniline, N,N-diethylaniline, etc.), piperidine, N-alkylpiperidine (e.g., N-methylpiperidine, 'N-ethylpiperidine, etc.), the lower alkali metal al
• the dye condensation reaction also can be advanta geously carried out in the presence of an inert diluent, e.g., pyridine.
• an inert diluent e.g., pyridine.
• suitable diluents which can be employed in addition to or in place of the conventionally employed pyridine include lower alkanols such as ethanol, n-propanol, isopropanol, n-butanol, etc., also dimethyl formamide, quinoline, 1,4-dioxane, etc.
• condensation reactions in the production of cyanine dyes are carried out under temperatures varying from below ambient temperature (ca. 25 C.) to the reflux temperature of the reaction mixture.
• suitable temperatures employed in the condensation reaction of the active methylene containing compound and the alkene urethane reactant varies from about 20 to 0, depending, of course, on the dye being produced.
• the reaction mixture is either chilled or drowned in an appropriate diluent to obtain the dye which is subsequently purified by conventional means.
• acetic anhydride is reacted with an anilino alkylene intermediate to produce a reactant which when reacted with the active methyl or methylene containing compound forms the desired dye.
• a reaction results in the elimination of acetanilide and similar simple materials.
• R, R R R X, Y, and Y and n have the values designated previously.
• suitable anilinoalkylene intermediate compounds which can be employed in accordance with this embodiment of the present invention wherein the alkene urethane reactant is produced in situ can comprise any and all of the precursors of the cyclic quarternary ammonium vinyl or polyvinyl urethanes and cyclic tertiary amidinium alkylene urethanes described above.
• reaction conditions including use of basic condensing catalysts and inert diluents are the same as those conventionally employed in the production of carbocyanine and related dyes.
• the present invention comprises an improvement associated with a conventional anilinoalkylene process of producing cyanine merocyanine and oxanol dyes.
• the improvement of the present invention comprises the utilization of an N-phenyl-N-vinyl urethane intermediate or an in situ prepared N-phenyl-N-vinyl urethane intermediate which through reaction with an active methyl containing compound will provide the desired dyestuft with minimum objectionable side reactions due to fragmentation, multiple condensation or decomposition associated with the use of conventional acetylanilino alkylene intermediates.
• the mixture was then poured into a solution of water (800 ml.) containing sodium perchlorate (16 g.), chilled and the residual gum triturated several times with hot Water.
• the dyes of Examples II and III were identical with the dye prepared by the conventional method which utilizes acetic anhydride in place of ethyl chloroformate.
• the yield of dye prepared by the conventional method averages only 3040% and is contaminated by difficult to remove by-products of reaction.
• the ethyl chloroformate method not only gives vastly improved yields but also results in a drastic reduction of undesirable side reactions, thereby producing a much cleaner product.
• the dye had the structure:
• the dye had the structure:
• the dye had the structure:
• the dye had the structure:
• the dye had the structure:
• the dye had the structure:
• the resultant gum was triturated several times with acetone (50 ml.) and then dissolved in hot acetic acid (75 1111.), Hydroehloric acid (3 ml.) was added and 16 the dye crystallized out. After cooling, the dye was collected by filtration and washed with acetone. The yield of dye after several methanol boilouts was 3.3 g. (69% of theory). This dye is identical with an authentic sample prepared by a conventional method.
• the dye had the structure:
• Example XII was repeated with the exception that the 2.6 g. of malonaldehyde dianil monohydrochloride was replaced by 2.9 g. of glutaconaldehyde dianil monohydrochloride was replaced by 2.9 g. of glutaconaldehyde dianil monohydrochloride.
• a dye having the following structure was obtained:
• the dye has the following structure:
• dyes produced in accordance with the process of the present invention are particularly useful for inclusion as sensitizers for photographic silver halide emulsions, in filter and antihalation layers, and as optical sensitizers for electrophotographic materials.
• dyes produced in accordance with the present invention are particularly applicable because in many instances by employing the improved process of the present invention, it is possible to directly produce photographic grade dyes. This, of course, is a distinct advantage over previously employed processes which have involved considerable purification techniques to produce dyes useful in photographic emulsions and other reprographic elements.
• Sensitization of the dyes employed in accordance with the process of the present invention is directed frequently to the ordinarily employed gelatino-silver halide emulsions.
• the dyes are advantageously ineorperated in the washed, finished emulsion and should, of course, be uniformly distributed throughout the emulsion.
• the methods of incorporating dyes in emulsion are simple and well known to those skilled in the art of emulsion making. It is convenient to add the dyes from solutions in appropriate solvents. The solvent must, of course, be compatible with the emulsion and substantially free from any deleterious effect on the light-sensitive materials.
• the concentration of the dyes when used as sensitizers in the emulsion can vary widely, i.e., from about to about 100 mgs. per liter of fiowable emulsion.
• the concentration of the dye will vary according to the type of actinic radiation-sensitive material in the emulsion and according to the effects desired.
• the suitable and most economical concentration for any given emulsion will be apparent to those skilled in the art upon making the ordinary tests and observations customarily used in the art of emulsion making.
• a quantity of the dye may be dissolved in ethanol or other suitable solvent and a volume of this solution containing from 5 to 100 mgs. of dye is slowly added to about 1000 cc. of a gelatino-silver-halide emulsion, with stirring. Stirring is continued until the dye is uniformly distributed throughout the emulsion.
• the ordinary gelatino-silver-bromide (including bromiodide) emulsions With fine-grain emulsions, which include most of the ordinarily employed gelatino-silver-chloride emulsions, somewhat larger concentrations of dye may be necessary to secure the optimum sensitizing effect.
• Photographic silver halide emulsions which can advantageously be sensitized by means of the dyes produced in accordance with the process of the present invention comprise the customarily employed gelatino-silver-chloride, gelatino silver chlorobromide, gelatino-silver-bromide, and gelatino-silver bromiodide developing-out emul- Photographic silver halide emulsions, such as those listed above, containing the sensitizing dyes of the present invention can also contain such addenda as chemical sensitizers, e.g., sulfur sensitizers (e.g., allylthiocarbamide, thiourea, allylisothiocyanate, cystine, etc.), various gold compounds (e.g., potassium chloroaurate, auric thichloride, etc.) (see US.
• chemical sensitizers e.g., sulfur sensitizers (e.g., allylthiocarbamide, thi
• color couplers such as those described in US. Pat. 2,423,730, Spense and Carroll, US. Pat. 2,640,776, etc.; or mixtures of such addenda.
• Dispersing agents for color couplers such as those set forth in US. Pats. 2,322,027 and 2,304,940, can also be employed in the above described emulsions.
• the present invention comprises an improved process for the production of conventional cyanine dyes, e.g., carbocyanine, merocyanine, oxanol and related dyes.
• conventional cyanine dyes e.g., carbocyanine, merocyanine, oxanol and related dyes.
• R is selected from the group consisting of alkyl, substituted alkyl, allyl heterocycloalkyl, and aralkyl groups of the type usual in cyanine dyes;
• X is an anion of the type usual in cyanine dyes; and
• Y represents the atoms necessary to complete a heterocyclic ring of the type usual in cyanine dyes;
• R being hydrogen when n is greater than 1; and R X,
• a process for the production of a merocyanine dye comprising condensing an active methyl containing compound of the formula:
• Y represents the atoms necessary to complete a heterocyclic nucleus of the type usual in merocyanine dyes
• R is selected from the group consisting of hydrogen, lower alkyl, lower hydroxyalkyl, lower carboxyalkyl, lower alkoxyalkyl, allyl and aralkyl groups, and n is an integer from 1-3, R being hydrogen when n is greater than I.
• a process for the production of a cyanine dye comprising:
• A-- has the structure 2 3 l I c c (CE CH) wherein R is selected from the group consisting of hydrogen, lower alkyl, aryl, aryloxy and arylthio groups, and R is selected from the group consisting of hydrogen, lower alkyl and aryl groups, at least one of said R and R being hydrogen; and n is an integer from 1 to 3, R being hydrogen when n is greater than 1; and (11) without isolation of the reaction product of I,
• a process for the production of a merocyanine dye comprising:
• Y represents the atoms necessary to complete a heterocyclic nucleus of the type usual in merocyanine dyes
• R is selected from the group consisting of hydrogen, lower alkyl, lower hydroxyalkyl, lower carboxyalkyl, lower alkoxyalkyl, allyl and aryl groups, and n is an integer from 1-3, R being hydrogen when n is greater than 1, and
• R is selected from the group consisting of lower alkyl, substituted alkyl, allyl, heterocycloalkyl and aralkyl groups of the type usual in cyanine dyes;
• X is an anion of the type usual in cyanine dyes; and
• Y represents the atoms necessary to complete a heterocyclic ring of the type usual in cyanine dyes.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Physics & Mathematics (AREA)
• General Physics & Mathematics (AREA)
• Plural Heterocyclic Compounds (AREA)

Applications Claiming Priority (1)

Publications (1)

Family

ID=25236833

Family Applications (1)

Country Status (7)

Cited By (1)

• 1969
  • 1969-05-07 US US822737A patent/US3646017A/en not_active Expired - Lifetime
• 1970
  • 1970-04-29 GB GB3062370*A patent/GB1310926A/en not_active Expired
  • 1970-05-04 CH CH663970A patent/CH569051A5/xx not_active IP Right Cessation
  • 1970-05-04 CH CH633473A patent/CH569052A5/xx not_active IP Right Cessation
  • 1970-05-05 DE DE19702021910 patent/DE2021910A1/de active Pending
  • 1970-05-05 FR FR7016388A patent/FR2047320A5/fr not_active Expired
  • 1970-05-06 BE BE750034D patent/BE750034A/xx unknown
  • 1970-05-07 CA CA082105A patent/CA924722A/en not_active Expired

Also Published As

Similar Documents